Canonical Allele Identifier: CA337804667
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949620G>C (hg19) chr1:g.1014240G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014240G>C , CM000663.2:g.1014240G>C GRCh38
NC_000001.10:g.949620G>C , CM000663.1:g.949620G>C GRCh37
NC_000001.9:g.939483G>C NCBI36
NG_033033.1:g.5774G>C
NG_033033.2:g.18103G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.236G>C ENSP00000485643.1:p.Arg79Thr
ENST00000649529.1:c.260G>C MANE Select ENSP00000496832.1:p.Arg87Thr
ENST00000379389.4:c.260G>C ENSP00000368699.4:p.Arg87Thr
ENST00000624652.1:c.236G>C ENSP00000485313.1:p.Arg79Thr
ENST00000624697.3:c.236G>C ENSP00000485643.1:p.Arg79Thr
NM_005101.3:c.260G>C NP_005092.1:p.Arg87Thr
NM_005101.4:c.260G>C MANE Select NP_005092.1:p.Arg87Thr
Search 100 bp 5'
Search 100 bp 3'